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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922809Generated: October 30, 2026

Methanol → Methyl 7-chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxylate

https://huagongshe.com/reaction/922809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHydrochloride methanolHCID 21893726—
Reactant7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrileHCID 89543584—
ProductMethyl 7-chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxylateHCID 8954385490%

Reaction Conditions

Temperature60 °C

Reaction Steps

7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile (4.4 g, 14.07 mmol) was suspended in MeOH (70.3 ml), added 200 ml sat HCl/MeOH and then heated to 60° C. for 4 hours. The reaction was allowed to cool to ambient temperature and then was concentrated. The residue was dissolved in EtOAc and then washed with 1:1 1N NaOH/sat NaHCO3, brine, dried (MgSO4) and concentrated to afford methyl 7-chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxylate (4.4 g, 12.73 mmol, 90% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278960B2
Source datasetuspto-grants-2016_03
ORD IDord-c4b00f3c03664dcaacf8cf11ca62f7bf
Source noteuspto-grants-2016_03